Division of Immunology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115, USA.
J Immunol. 2010 Nov 15;185(10):5683-7. doi: 10.4049/jimmunol.1001974. Epub 2010 Oct 20.
EWS/FLI1-activated transcript 2 (EAT-2)A and EAT-2B are single SH2-domain proteins, which bind to phosphorylated tyrosines of signaling lymphocyte activation molecule family receptors in murine NK cells. While EAT-2 is a positive regulator in human cells, a negative regulatory role was attributed to the adapter in NK cells derived from EAT-2A-deficient 129Sv mice. To evaluate whether the genetic background or the presence of a selection marker in the mutant mice could influence the regulatory mode of these adapters, we generated EAT-2A-, EAT-2B-, and EAT-2A/B-deficient mice using C57BL/6 embryonic stem cells. We found that NK cells from EAT-2A- and EAT-2A/B-deficient mice were unable to kill tumor cells in a CD244- or CD84-dependent manner. Furthermore, EAT-2A/B positively regulate phosphorylation of Vav-1, which is known to be implicated in NK cell killing. Thus, as in humans, the EAT-2 adapters act as positive regulators of signaling lymphocyte activation molecule family receptor-specific NK cell functions in C57BL/6 mice.
EWS/FLI1 激活转录因子 2(EAT-2)A 和 EAT-2B 是单一的 SH2 结构域蛋白,可与信号淋巴细胞激活分子家族受体在鼠 NK 细胞中的磷酸化酪氨酸结合。虽然 EAT-2 在人类细胞中是一种正调节剂,但在 EAT-2A 缺陷的 129Sv 小鼠来源的 NK 细胞中,该衔接蛋白被认为具有负调节作用。为了评估遗传背景或突变小鼠中选择标记的存在是否会影响这些衔接蛋白的调节模式,我们使用 C57BL/6 胚胎干细胞生成了 EAT-2A、EAT-2B 和 EAT-2A/B 缺陷型小鼠。我们发现,EAT-2A-和 EAT-2A/B 缺陷型小鼠的 NK 细胞无法以 CD244 或 CD84 依赖性方式杀死肿瘤细胞。此外,EAT-2A/B 正向调节 Vav-1 的磷酸化,Vav-1 已知与 NK 细胞杀伤有关。因此,与人类一样,EAT-2 衔接蛋白在 C57BL/6 小鼠中作为信号淋巴细胞激活分子家族受体特异性 NK 细胞功能的正调节剂发挥作用。